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1.
Dalton Trans ; 53(24): 10270-10284, 2024 Jun 17.
Article in English | MEDLINE | ID: mdl-38829264

ABSTRACT

The synthesis of eight Ru(II) and Os(II) photosensitizers bearing a common 9,10-disubstituted-1,4,5,8-tetraazaphenanthrene backbone is reported. With Os(II) photosensitizers, the 9,10-diNH2-1,4,5,8-tetraazaphenanthrene could be directly chelated onto the metal center via the heteroaromatic moiety, whereas similar conditions using Ru(II) resulted in the formation of an o-quinonediimine derivative. Hence, an alternative route, proceeding via the chelation of 9-NH2-10-NO2-1,4,5,8-tetraazaphenanthrene and subsequent ligand reduction of the corresponding photosensitizers was developed. Photosensitizers chelated via the polypyridyl-type moiety exhibited classical photophysical properties whereas the o-quinonediimine chelated Ru(II) analogues exhibited red-shifted absorption (520 nm) and no photoluminescence at room temperature in acetonitrile. The most promising photosensitizers were investigated for excited-state quenching with guanosine-5'-monophosphate in aqueous buffered conditions where reductive excited-state electron transfer was observed by nanosecond transient absorption spectroscopy.

2.
J Am Chem Soc ; 146(15): 10286-10292, 2024 Apr 17.
Article in English | MEDLINE | ID: mdl-38569088

ABSTRACT

Excited-state quenching and reduction of [Fe(phtmeimb)2]+, where phtmeimb is phenyl[tris(3-methyl-imidazolin-2-ylidene)]borate, with iodide, bromide, and chloride were studied in dichloromethane, acetonitrile, and acetonitrile/water 1:1 mixture by means of steady-state and time-resolved spectroscopic techniques. Quenching rate constants were almost diffusion-limited in dichloromethane and acetonitrile and followed the expected periodic trend, i.e., I- > Br- > Cl-. Confirmation of excited-state reductive electron transfer was only unambiguously obtained when iodide was used as a quencher. The cage escape yields, i.e., the separation of the geminate radical pair formed upon bimolecular excited-state electron transfer, were determined. These yields were larger in dichloromethane (0.079) than in acetonitrile (0.017), and no photoproduct could be observed in acetonitrile/water 1:1. This study further emphasizes that solvents with low dielectric constant are more suited for productive excited-state electron transfer using Fe(III) photosensitizers with 2LMCT excited state.

3.
Inorg Chem ; 62(39): 16196-16202, 2023 Oct 02.
Article in English | MEDLINE | ID: mdl-37734153

ABSTRACT

Two iridium(III) binuclear photosensitizers, [Ir(dFCF3ppy)2(N-N)Ir(dFCF3ppy)2]2+, where N-N is tetrapyrido[3,2-a:2',3'-c:3″,2″-h:2‴,3‴-j]phenazine (Ir-TPPHZ) and 1,4,5,8-tetraazaphenanthrene[9,10-b]-1,4,5,8,9,12-hexaazatriphenylene (Ir-TAPHAT) are reported for iodide, bromide, and chloride photooxidation in acetonitrile and acetonitrile/water mixtures using blue-light irradiation. Excited-state reduction potentials Ered* of +2.02 and +2.09 V vs NHE were determined for Ir-TPPHZ and Ir-TAPHAT, respectively. Both photosensitizers' excited states were efficiently quenched by iodide, bromide, and chloride with quenching rate constants in the (3.5-9.2) × 1010 and (0.0036-2.9) × 1010 M-1 s-1 ranges in neat acetonitrile and acetonitrile/water mixtures, respectively. Nanosecond transient absorption spectroscopy provided unambiguous evidence of reductive excited-state electron transfer, with all halides in the solvent mixtures containing up to 50% water. Cage-escape yields were large (55-96%) in acetonitrile and dropped below 32% in 50:50 acetonitrile/water mixtures.

4.
STAR Protoc ; 4(2): 102312, 2023 May 13.
Article in English | MEDLINE | ID: mdl-37182202

ABSTRACT

Here, we present a protocol for the determination of cage-escape yields following excited-state electron transfer between a photosensitizer and a quencher. We describe steps for determining changes in molar absorption coefficient of the different oxidation states via photolysis experiments and the percentage of reacted species via steady-state or time-resolved spectroscopy. We then detail measurement of the amount of formed product via nanosecond transient absorption spectroscopy. For complete details on the use and execution of this protocol, please refer to Ripak et al. (2023).1.

5.
Chem Catal ; 3(2)2023 Feb 16.
Article in English | MEDLINE | ID: mdl-36936750

ABSTRACT

Aryl diazonium salts are ubiquitous building blocks in chemistry, as they are useful radical precursors in organic synthesis as well as for the functionalization of solid materials. They can be reduced electrochemically or through a photo-induced electron transfer reaction. Here we provide a detailed picture of the ground and excited-state reactivity of a series of 9 rare and earth abundant photosensitizers with 13 aryl diazonium salts, which also included 3 macrocyclic calix[4]arene tetradiazonium salts. Nanosecond transient absorption spectroscopy confirmed the occurrence of excited-state electron transfer and was used to quantify cage-escape yields, i.e. the efficiency with which the formed radicals separate and escape the solvent cage. Cage-escape yields were large; increased when the driving force for photo-induced electron transfer increased and also tracked with the C-N2 + bond cleavage propensity, amongst others. A photo-induced borylation reaction was then investigated with all the photosensitizers and proceeded with yields between 9 and 74%.

6.
Chem Commun (Camb) ; 58(58): 8057-8060, 2022 Jul 19.
Article in English | MEDLINE | ID: mdl-35699027

ABSTRACT

Picosecond optical and X-ray absorption spectroscopies with time-dependent density functional theory revealed the reaction pathways, electronic and structural conformations of Ir-Co hydrogen evolution photocatalysts. The dyad bearing 2-phenylpyridine ancillary ligands produced more photoreduced Co(II) than its 2-phenylisoquinoline analogue. These findings are important for designs of earth-abundant photosensitizers for photocatalytic applications.


Subject(s)
Iridium , Organometallic Compounds , Cobalt , Electronics , Hydrogen/chemistry , Iridium/chemistry , Kinetics , Models, Molecular , Organometallic Compounds/chemistry
7.
Photochem Photobiol Sci ; 21(8): 1433-1444, 2022 Aug.
Article in English | MEDLINE | ID: mdl-35595935

ABSTRACT

A series of nine [Ir(piq)2(LL)]+.PF6- photosensitizers, where piqH = 1-phenylisoquinoline, was developed and investigated for excited-state electron transfer with sacrificial electron donors that included triethanolamine (TEOA), triethylamine (TEA) and 1,3-dimethyl-2-phenyl-2,3-dihydro-1H-benzo[d]imidazole (BIH) in acetonitrile. The photosensitizers were obtained in 57-82% yield starting from the common [Ir(piq)2µ-Cl]2 precursor and were all characterized by UV-Vis absorption as well as by steady-state, time-resolved spectroscopies and electrochemistry. The excited-state lifetimes ranged from 250 to 3350 ns and excited-state electron transfer quenching rate constants in the 109 M-1 s-1 range were obtained when BIH was used as electron donor. These quenching rate constants were three orders of magnitude higher than when TEA or TEOA was used. Steady-state photolysis in the presence of BIH showed that the stable and reversible accumulation of mono-reduced photosensitizers was possible, highlighting the potential use of these Ir-based photosensitizers in photocatalytic reactions relevant for solar fuels production.


Subject(s)
Photosensitizing Agents , Photolysis , Photosensitizing Agents/chemistry
8.
Chemistry ; 28(42): e202201220, 2022 Jul 26.
Article in English | MEDLINE | ID: mdl-35608397

ABSTRACT

Controlling redox activity of judiciously appended redox units on a photo-sensitive molecular core is an effective strategy for visible light energy harvesting and storage. The first example of a photosensitizer - electron donor coordination compound in which the photoinduced electron transfer step is used for light to electrical energy conversion and storage is reported. A photo-responsive Ru-diimine module conjugated with redox-active catechol groups in [Ru(II)(phenanthroline-5,6-diolate)3 ]4- photosensitizer can mediate photoinduced catechol to dione oxidation in the presence of a sacrificial electron acceptor or at the surface of an electrode. Under potentiostatic condition, visible light triggered current density enhancement confirmed the light harvesting ability of this photosensitizer. Upon implementation in galvanostatic charge-discharge of a Li battery configuration, the storage capacity was found to be increased by 100 %, under 470 nm illumination with output power of 4.0 mW/cm-2 . This proof-of-concept molecular system marks an important milestone towards a new generation of molecular photo-rechargeable materials.

9.
Inorg Chem ; 61(13): 5245-5254, 2022 Apr 04.
Article in English | MEDLINE | ID: mdl-35325530

ABSTRACT

Two new cyclometalated Ir(III) diimine complexes were used as photosensitizers for homogeneous hydrogen evolution reaction (HER). These complexes were characterized by electrochemistry, ultraviolet-visible absorption, time-resolved and steady-state photoluminescence spectroscopy as well as by theoretical methods. The metal-ligand-to-ligand charge transfer character of their lowest excited state was shown to be competent for efficient H2 photoproduction in the presence of [Co(dmgH)2(py)Cl] as the hydrogen evolution catalyst, triethanolamine as the sacrificial electron donor, and HBF4 as the proton source. Under optimized experimental conditions, both complexes displayed HER over a period of more than 90 h, with turnover numbers reaching up to 11,650, 10,600, and 174 molH2 molPS-1 under blue-, green-, and red-light irradiation, respectively. Both complexes showed higher stability and efficiency vs HER than most of the previously described systems of the same kind.

10.
ChemSusChem ; 13(9): 2225-2231, 2020 May 08.
Article in English | MEDLINE | ID: mdl-32059070

ABSTRACT

1,10-Phenanthroline-5,6-dione (phendione)-based transition-metal complexes are known for their use in pharmacological and catalysis applications. However, their application in electrochemical energy storage has not been investigated thus far. Herein, the feasibility of employing phendione-transition-metal complexes was investigated for electrochemical charge storage by taking advantage of the reversible redox activity of both carbonyl groups and transition metal center, contributing to augmented charge storage. Interestingly, the chemistry of the counter ion in the studied complexes effectively tuned the solubility and improved the cycling stability. Although further studies are required to limit the solubility and active-species shuttle, this study explores the bottlenecks of phendione-transition-metal complexes as electrode materials for solid-electrode-format batteries.

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